The present invention describes compositions and methods comprising lactic acid-producing bacteria in baked goods.

Patent
   10383342
Priority
Aug 29 2007
Filed
Aug 27 2008
Issued
Aug 20 2019
Expiry
Aug 27 2028
Assg.orig
Entity
Large
0
189
currently ok
11. A chemically leavened baked muffin comprising an edible starch and isolated bacillus coagulans spores, wherein said isolated bacillus coagulans spores in the muffin are viable and germination-competent after baking.
1. A chemically leavened baked muffin comprising an edible starch and isolated bacillus coagulans spores, wherein said isolated bacillus coagulans spores comprise gbi-30 strain (ATCC Designation No. PTA-6086) spores,
wherein the bacillus coagulans spores in the muffin are viable and germination-competent after baking.
2. A method of making a chemically leavened baked muffin comprising:
providing a flour containing base mix and a liquid portion of water;
mixing said flour containing base mix and said water to form a batter;
adding isolated bacillus coagulans bacteria to said batter, wherein said isolated bacillus coagulans bacteria comprise gbi-30 strain (ATCC Designation No. PTA-6086) bacteria, and wherein said isolated bacillus coagulans bacteria comprise at least 95% spores; and
heat processing said batter to produce a baked good,
thereby making said muffin, wherein said isolated bacillus coagulans bacteria in said muffin comprise at least 95% spores, and wherein the spores are viable and germination-competent after heat processing.
3. The method of claim 2, wherein said isolated bacillus coagulans bacteria comprise between 1% and 10% by weight of said muffin.
4. The muffin of claim 1, further comprising a fat selected from the group consisting of oil, butter, shortening, artificial lipid, synthetic fat, and a fat substitute.
5. The muffin of claim 1, further comprising a sugar, sugar substitute, or artificial sweetener.
6. The muffin of claim 1, wherein said muffin is a blueberry bran muffin.
7. The method of claim 2, wherein said muffin is a blueberry bran muffin.
8. The muffin of claim 1, wherein said isolated bacillus coagulans spores were impregnated into the muffin in an amount of about 1×106 to about 1×1010 CFU per gram of the muffin before baking.
9. The muffin of claim 8, wherein said isolated bacillus coagulans spores were impregnated into the muffin in an amount of about 1×106 to about 1×108 CFU per gram of the muffin before baking.
10. The method of claim 2, wherein said isolated bacillus coagulans bacteria is added to said batter in an amount of about 1×106 to about 1×108 CFU per gram.

This application claims the benefit of U.S.S.N. 60/966,897, filed Aug. 29, 2007, which is incorporated herein by reference in its entirety.

The present invention relates to the use of lactic acid-producing bacteria in baked goods.

The gastrointestinal microflora plays a number of vital roles in maintaining gastrointestinal tract function and overall physiological health. The growth and metabolism of the many individual bacterial species inhabiting the gastrointestinal tract depend primarily upon the substrates available to them, most of which are derived from the diet. (See e.g., Gibson G. R. et al., 1995. Gastroenterology 106: 975-982; Christl, S. U. et al., 1992. Gut 33: 1234-1238). These findings have led to attempts to modify the composition and metabolic activities of the bacterial community through diet, primarily with probiotics, which are live microbial food supplements.

Probiotic organisms are non-pathogenic, non-toxigenic, retain viability during storage, and survive passage through the stomach and small intestine. Since probiotics do not generally permanently colonize the host, they need to be ingested regularly for any health promoting properties to persist.

The invention describes the use of acid-producing bacteria in baked goods for human or animal consumption. Specifically, the invention provides compositions comprising a baked composition of an edible starch and an isolated Bacillus coagulans bacterium and methods of administering probiotic bacterial spores to a human or other animal by providing a baked good containing the spores to the human or other animal whereby the human or animal ingests the baked good and the spores germinate in the gastrointestinal tract (stomach or small intestine). Germination of spores and/or colonization of gastrointestinal tissue by the administered bacterial spores or cells is assessed by detecting the probiotic microorganism in the stool of the individual.

An exemplary baked good includes a bread, a cake, a pie, a tart, a pastry, a candy bar, an energy bar, a food bar, granola, a granola bar, a quiche, a cookie, cereal, a pizza, a corn chip, a tortilla chip, a potato chip, a baked cracker, a dehydrated vegetable, a dehydrated fruit, or a treat for companion animals. In another aspect, the baked good includes any good comprising flour. In yet another aspect, the baked good of the invention includes any good that is heated, e.g., baked (exposure of dry heat). Preferably, the baked good is a muffin. In one aspect, the baked good is a blueberry bran muffin.

Optionally, the baked composition also includes a fat. Suitable fats include oils, butters, shortenings, artificial lipids, synthetic fats, and a fat substitutes. In another aspect, the baked composition also includes a sugar, sugar substitute, or artificial sweetener.

In one aspect, the isolated Bacillus coagulans comprise between about 0.01% to about 50% by weight of the baked good. Optionally, the isolated Bacillus coagulans comprise between about 0.01% and about 10% by weight of the baked good. Preferably, the isolated Bacillus coagulans comprise between about 0.01% and about 0.1% by weight of the baked good.

The invention also provides bacterial species including Bacillus coagulans, e.g., Bacillus coagulans hammer, preferably Bacillus coagulans hammer strain Accession No. ATCC 31284, or one or more strains derived from Bacillus coagulans hammer strain Accession No. ATCC 31284 (e.g., ATCC Numbers: GBI-20, ATCC Designation Number PTA-6085; GBI-30, ATCC Designation Number PTA-6086; and GBI-40, ATCC Designation Number PTA-6087; see U.S. Pat. No. 6,849,256 to Farmer).

Optionally, the isolated Bacillus coagulans is in the form of a spore. Alternatively, the isolated Bacillus coagulans is in the form of a vegetative cell. In another aspect, the isolated Bacillus coagulans is in the form of a mixture of vegetative cells and spores.

The invention also provides for methods of making a baked good, wherein the baked good comprises a flour containing base mix and a liquid portion of water. Optionally, the method includes providing a flour containing base mix and a liquid portion of water; mixing the flour containing base mix and water to form a batter or dough; applying an isolated Bacillus coagulans bacterium to the batter or dough, and heat processing the batter or dough to cook the baked good. Alternatively, the method includes providing a flour containing base mix and a liquid portion of water; mixing the flour containing base mix and water to form a batter or dough; combining an isolated Bacillus coagulans bacterium with the batter or dough, and heat processing the batter or dough to cook the baked good.

Optionally, the isolated Bacillus coagulans is Bacillus coagulans hammer strain Accession No. ATCC 31284. In an exemplary embodiment, the isolated Bacillus coagulans is GBI-30 strain (ATCC Designation Number PTA-6086). In one aspect, the isolated Bacillus coagulans is in the form of a spore. Alternatively, the isolated Bacillus coagulans is in the form of a vegetative cell. In a preferred embodiment, the isolated Bacillus coagulans comprise between 1% and 10% by weight of the baked good.

The invention also provides compositions comprising a dry mix for baked goods including a flour and an isolated Bacillus coagulans bacterium.

The Bacillus coagulans Hammer strains of the invention are non-pathogenic and generally regarded as safe for use in human nutrition (i.e., GRAS classification) by the U.S. Federal Drug Administration (FDA) and the U.S. Department of Agriculture (USDA), and by those skilled in the art. Furthermore, the Bacillus coagulans Hammer strains of the invention germinate at or below human body temperature, rendering them useful as probiotics. Many Bacillus coagulans strains outside the Hammer group have mostly industrial applications, little or no nutritional benefit, and environmental contaminants that have not been evaluated for safety. Moreover, many other non-Hammer strains of Bacillus coagulans grow optimally at temperatures that exceed human body temperature and, thus, do not germinate efficiently in the human body. Such strains are less or not suitable as probiotics for human consumption.

Cited publications are incorporated herein by reference. Both the foregoing general description and the following detailed description and examples are exemplary and explanatory only and are not restrictive of the invention as claimed.

The present invention is directed to the discovery that non-pathogenic lactic acid-producing bacteria (i.e., “lactic acid bacteria”), such as the exemplary Bacillus coagulans, are useful in baked compositions as a probiotic.

Probiotic Lactic Acid-Producing Bacteria

A probiotic lactic acid-producing bacteria suitable for use in the methods and compositions of the invention produces acid and is non-pathogenic. There are many suitable bacteria identified as described herein, although the invention is not limited to currently known bacterial species insofar as the purposes and objectives of the bacteria is described. The property of acid production is important to the effectiveness of the probiotic lactic acid-producing bacteria of this invention.

The invention provides using a lactic acid-producing bacteria, such as a spore-forming Bacillus species, such as B. coagulans. Preferably, the spore-forming Bacillus species of the invention is B. coagulans Hammer.

Exemplary methods and compositions are described herein using Bacillus coagulans as a probiotic. Purified and/or isolated Bacillus coagulans is particularly useful as a probiotic in baked edible food products. Probiotic B. coagulans is non-pathogenic and is generally regarded as safe (i.e., GRAS classification) by the U.S. Federal Drug Administration (FDA) and the U.S. Department of Agriculture (USDA), and by those skilled in the art.

Bacillus coagulans is a non-pathogenic gram positive spore-forming bacteria that produces L(+) lactic acid (dextrorotatory) in fermentation conditions. It has been isolated from natural sources, such as heat-treated soil samples inoculated into nutrient medium (Bergey's Manual off Systemic Bacteriology, Vol. 2, Sneath, P. H. A., et al., eds., Williams & Wilkins, Baltimore, Md., 1986). Purified B. coagulans strains have served as a source of enzymes including endonucleases (e.g., U.S. Pat. No. 5,200,336); amylase (U.S. Pat. No. 4,980,180); lactase (U.S. Pat. No. 4,323,651); and cyclo-malto-dextrin glucano-transferase (U.S. Pat. No. 5,102,800). B. coagulans has been used to produce lactic acid (U.S. Pat. No. 5,079,164). A strain of B. coagulans (referred to as L. sporogenes; Sakaguti & Nakayama (ATCC 31284)) has been combined with other lactic acid producing bacteria and B. natto to produce a fermented food product from steamed soybeans (U.S. Pat. No. 4,110,477).

Bacterial species include Bacillus coagulans, e.g., Bacillus coagulans hammer, preferably Bacillus coagulans hammer strain Accession No. ATCC 31284, or one or more strains derived from Bacillus coagulans hammer strain Accession No. ATCC 31284 (e.g., ATCC Numbers: GBI-20, ATCC Designation Number PTA-6085; GBI-30, ATCC Designation Number PTA-6086; and GBI-40, ATCC Designation Number PTA-6087; see U.S. Pat. No. 6,849,256 to Farmer).

Bacillus coagulans was previously mis-characterized as a Lactobacillus and labeled as Lactobacillus sporogenes (See Nakamura et al. 1988. Int. J. Syst. Bacteriol. 38: 63-73). However, initial classification was incorrect because Bacillus coagulans produces spores and excretes L(+)-lactic acid through metabolism. Both of these characteristics provide key features to the utility of Bacillus coagulans. These developmental and metabolic aspects required that the bacterium be classified as a lactic acid Bacillus. In addition, it is not generally appreciated that classic Lactobacillus species are unsuitable for colonization of the gut due to their instability in the harsh (i.e., acidic) pH environment of the bile, particularly human bile. By contrast, Bacillus coagulans is able to survive and colonize the gastrointestinal tract in the bile environment and even grown in this low pH range.

Probiotic Activity of Bacillus coagulans

It is well-documented clinically that many species of bacterial, mycotic and yeast pathogens possess the ability to cause a variety of gastrointestinal disorders including, but not limited to: disruption of normal gastrointestinal biochemical function, necrosis of gastrointestinal tissues, and disruption of the bioabsorption of nutrients, and like conditions. The probiotic microorganism-containing compositions of the present invention inhibit these pathogens. Thus, the compositions of the invention are useful in the prophylactic or therapeutic treatment of conditions associated with infection by these aforementioned pathogens.

In one aspect, a Bacillus coagulans strain is included in the composition in the form of vegetative cells. Alternatively, the Bacillus coagulans strain is included in the composition in the form of spores. The invention also provides for including the Bacillus coagulans strain in the composition in the form of a dried cell mass, a stabilized paste, or a stabilized gel.

Because Bacillus spores are heat and pressure-resistant and can be stored as a dry power, they are particularly useful for formulation into and manufacture of products such as the various baked products and compositions described herein. A Bacillus species is well suited for the present invention, particularly species having the ability to form spores which are relatively resistant to heat and other conditions, making them ideal for storage (shelf-life) in product formulations.

The Bacillus coagulans of the invention survives storage (shelf-life) from about 12 days to about 2 years; from about 1 month to about 18 months; from about 3 months to about 1 year; or from about 6 months to about 9 months. For example, spores baked into a muffin remain viable and germination-competent for the self-life of the muffin (e.g., 6-12 days).

Micro-Encapsulation

In one aspect, the lactic-acid producing bacteria are incorporated into a microcapsule coating prior to addition to the baked good, using any micro-encapsulation process well-known in the art. The isolated Bacillus coagulans are packaged, or encapsulated, within another material in order to protect the bacteria from the surrounding environment. The capsules of the invention range in size from one-thousandth of a millimeter to seven millimeters. The internal ingredients of the microcapsule are released from their shells in various ways, including mechanical rupture of the capsule wall, dissolution of the wall, melting of the wall and diffusion through the wall. Thus, micro-encapsulation provides additional protection to the isolated Bacillus bacterium during heat processing (baking) of the baked goods of the invention. Physical methods of micro-encapsulation include pan coating, air-suspension coating, centrifugal extrusion, vibrational nozzle, and spray-drying. Chemical methods of micro-encapsulation include interfacial polymerization, in-situ polymerization, and matrix polymerization.

Alternatively, the lactic-acid producing bacteria is added to the baked good without micro-encapsulation.

Baked Goods

The invention is directed to the surprising discovery that lactic acid-producing bacteria, particularly Bacillus species, remain viable and retain their beneficial probiotic properties in heated/cooked baked goods, as the baked goods of the invention are heated to between about 300° F. to about 475° F. for about 5 minutes; about 10 minutes; about 30 minutes; or about 1 hour. In one aspect, the baked goods of the invention are heated up to about 350° F. for about 14 minutes; about 450° F. for about 17 minutes; or about 475° F. for about 6 minutes. The preferred heat and duration will vary depending upon the particular baked good. In one aspect, muffins are heated up to about 350° F. to about 375° F. for about 14 to about 20 minutes. In another aspect, cereal is heated up to about 475° F. for about 6 minutes.

As discussed further, the compositions are formulated in many configurations because the bacterium is present as a vegetative cell or as a spore, or both, depending on the species and form of the probiotic organism. The cells/spores are present in a variety of compositions suited for use in a baked good. In one aspect, the bacterium is present as a mixture of spores and vegetative cells. Preferably, the bacterium is present as at least 90% spores, e.g., 95%, 98%, or 99% spores.

An exemplary baked good includes a bread, a cake, a pie, a tart, a pastry, a candy bar, an energy bar, granola, a granola bar, a quiche, a cookie, cereal, a food bar, a pizza, a corn chip, a tortilla chip, a potato chip, a baked cracker, a dehydrated vegetable, or a treat for companion animals. In another aspect, the baked good includes any good comprising flour. In yet another aspect, the baked good of the invention includes any good that is heated. The invention provides for baked compositions baked/cooked in an oven. The compositions described herein are baked, or dried by subjecting them to heat. Alternatively, the baked compositions are steam-heated using high heat and excessive moisture, e.g., from about 10% to about 50% w/w water/dough prior to baking. Preferably, the baked composition comprises about 30-50% w/w water/dough; about 15-30% w/w water/dough; or about 5-15% w/w water/dough prior to baking. The invention also provides for confectionary compositions such as sweets, lollipops, candy bars, chocolate, and other sweet items of snack food.

Bread consists minimally of flour and water; salt is present in most cases, and usually a leavening agent such as yeast is used; however, any well-recognized method of making bread is used in the present invention. Optionally, the flour is wheat flour, rice four, corn flour, rye flour, potato flour, millet flour, baking flour, graham flour or quinoa flour. In one aspect, the flour is self-rising or self-raising flour. In some cases, bread also contains some amounts of sugar, spices, fruit (such as raisins, pumpkins, bananas, strawberries, blueberries, and the like), vegetables (such as onion or zucchini, and the like), nuts, or seeds (such as caraway, sesame or poppy seeds). Optionally, a fat such as an oil (vegetable oil, corn oil, olive oil, grape seed oil, nut oil or fruit oil), butter, shortening, artificial lipid, synthetic fat, or a fat substitute such as olestra is also present. In yet another aspect, a sugar, sugar substitute, or artificial sweetener such as saccharin, sucralose or aspartame is present. Suitable baked goods include, but are not limited to, buns, rolls, bagels, cookies, and pastries. Preferably, the baked good is a blueberry bran muffin.

The Bacillus bacterium is impregnated into the baked good during the manufacturing process of the baked good (e.g., added to the batter or dough mix). The pressure and heat resistance of Bacillus spores makes them particularly suitable for incorporation into the baked good prior to heat processing (baking) to cook the baked good.

In one aspect, the probiotic lactic acid-producing bacteria is introduced into or onto portions of the baked good by applying a composition containing viable bacteria to the baked good during a stage of the manufacture of the baked good. Preferably, the spores and/or vegetative cells of the probiotic acid-producing bacteria are introduced into batter or dough prior to baking the baked good. Alternatively, the bacteria is added during the baking process or after the baking process has concluded.

Preferably, the Bacillus bacterium is introduced into the batter prior to cooking the baked good. The invention provides a batter comprising a liquid mixture, usually based on one or more flours combined with liquids, such as water, milk or beer. In one aspect, egg is included in the batter. Optionally, a leavening agent is included in the mixture to aerate and fluff-up the batter as it cooks. In one embodiment, the viscosity of batter is very “stiff” (adhering to an upturned spoon). Alternatively, the viscosity of the batter is very “thin” (similar to single cream). Preferably, heat is applied to the batter by baking, in order to cook the ingredients (thus rendering them palatable) and to “set” the batter into a solid form. Following the baking process, the baked product is suitable for immediate human or animal consumption or for freezing, i.e., to store the product for future consumption.

The invention also provides for applying the Bacillus bacterium to a baked good using any of a variety of known methods including, for example, applying a powder, spray-drying the probiotic onto the baked good or soaking the baked good in a solution containing the probiotic. Optionally, the Bacillus bacterium is applied prior to cooking the baked good. Alternatively, the Bacillus bacterium is applied during or after the baking process has been completed.

The invention provides for a variety of methods for placing the bacterial composition onto a baked good. However, preferred methods include a “spray-dry” method in which the baked good is exposed in a low humidity chamber to an atomized mix containing a liquid composition, where the chamber is subsequently exposed to approximately 80-110° F. to dry the liquid, thereby impregnating the material of the baked good with the components of the composition.

A typical concentration is from approximately 1×107 to 1×1012 CFU; 1×108 to 1×1011 CFU; or 1×109 to 1×1010 CFU of viable bacterium or spores/in2 of external surface of baked good. Following drying, the baked good is ready for immediate use, storage in a sterile package, or for freezing.

The active ingredients (i.e., live bacteria or extracellular components), comprise about 0.01% to about 50% by weight of the final composition, preferably 0.01% to 10% by weight of the final baked good. Preferably, the isolated Bacillus coagulans comprise between about 0.01% and about 0.1% by weight of the baked good.

In one aspect, the amount of bacteria is about 104 to 1014 colony forming units (CFU) of bacteria per gram of baked good (i.e., vegetative cells and/or bacterial spores), preferably 105 to 1013 CFU/g. More preferably, the concentrations are 108 to 1013 CFU/g; 109 to 1012 CFU/g; or 1010 to 1011 CFU/g. In one aspect, the amount of bacteria is about 1×106 CFU per baked good. Alternatively, the amount of bacteria is about 2×1010 CFU/5 lbs of batter. The actual amount in a composition will vary depending upon the amounts of composition to be dispersed into the baked good and upon routes of dispersal.

In one aspect, the isolated Bacillus coagulans comprise between about 0.01% to about 10%; 0.01% to about 1%; or about 0.05% to about 0.1% by weight of the baked good. Optionally, the isolated Bacillus coagulans comprise about 1 mg to about 10 g; about 10 mg to about 1 g; or about 25 mg to about 75 mg by weight of the baked good.

In one aspect, the finished baked good is frozen and stored in a sterile package prior to consumption. The invention also provides for storing the baked good in a sterile package at room temperature prior to consumption. Alternatively, the baked goods are consumed immediately. In one aspect, the Bacillus coagulans spores survive storage (shelf-life), i.e., retain viability or the ability to germinate at physiological conditions (e.g., ingestion), from about 12 days to about 2 years; from about 1 month to about 18 months; from about 3 months to about 1 year; or from about 6 months to about 9 months. In one aspect, the Bacillus coagulans of the invention survives storage (shelf-life) in muffins for at least about 12 days. In another aspect, the Bacillus coagulans of the invention survives storage (shelf-life) in frozen pizza for at least about 2 years. In yet another aspect, the Bacillus coagulans of the invention survives storage (shelf-life) in food bars for at least about 6 to at least about 18 months.

Bacillus coagulans Hammer bacteria (ATCC Accession No. 31284) was inoculated and grown to a cell density of about 108 to 109 cells/ml in nutrient broth containing 5 g Peptone, 3 g Meat extract, 10-30 mg MnSO4, and 1,000 ml distilled water, adjusted to pH 7.0, using a standard airlift fermentation vessel at 30° C. The range of MnSO4 acceptable for sporulation is 1 mg/l to 1 g/l. The vegetative cells can actively reproduce up to 45° C., and the spores are stable up to 90° C. After fermentation, the B. coagulans bacterial cells or spores are collected using standard methods (e.g., filtration, centrifugation) and the collected cells and spores can be lyophilized, spray-dried, air-dried or frozen. As described herein, the supernatant from the cell culture is collected and used as an extracellular agent secreted by B. coagulans.

A typical yield from the above culture is in the range of about 109 to 1010 viable spores and more typically about 100 to 150 billion cells/spores per gram before drying. Spores maintain at least 90% viability after drying when stored at room temperature for up to ten years, and thus the effective shelf life of a composition containing B. coagulans Hammer spores at room temperature is about 10 years.

A culture of dried B. coagulans spores was prepared as follows. Ten million spores were inoculated into a one liter culture containing 24 g potato dextrose broth, 10 g of enzymic-digest of poultry and fish tissue, 5 g of FOS and 10 g MnSO4. The culture was maintained for 72 hours under a high oxygen environment at 37° C. to produce culture having about 150 billion cells per gram of culture. Thereafter, the culture was filtered to remove culture medium liquid, and the bacterial pellet was resuspended in water and freeze-dried. The freeze-dried powder is then ground to a fine powder using standard good manufacturing practice (GMP).

GBI-30, ATCC Designation Number PTA-6086, was microencapsulated (Maxx Performance; Chester, N.Y.) and added in dry powder form to blueberry bran muffin batter. The final concentration of Bacillus coagulans (both vegetative cells and spores) in the batter was about 20 billion (2×1010) CFU/5 lbs of batter (yield about 20 muffins). The final concentration of Bacillus coagulans (both vegetative cells and spores) in each muffin was about 1 billion (1×106) CFU/muffin. The isolated Bacillus coagulans comprised about 50 mg by weight per four ounce muffin. The muffins were cooked at 350° F. for 15 minutes. Subsequently, the muffins were frozen and stored at 0° F. for 14 days. The muffins were then thawed, crushed, and the number of viable bacteria was determined. Unexpectedly, approximately 41% of the bacteria in the muffin were viable after the above-mentioned cooking and freezing cycle.

Farmer, Sean, Lefkowitz, Andrew R., Bush, Michael, Maske, David

Patent Priority Assignee Title
Patent Priority Assignee Title
3091572,
3840684,
4110477, May 13 1977 Kabushiki Kaisha Naruse Fermentation Laboratory Method for producing natto containing lactic acid bacteria
4144346, Jan 31 1977 Janssen Pharmaceutica N.V. Novel 1-(1,3-dioxolan-2-ylmethyl)-1H-imidazoles
4278690, Sep 13 1978 Method of producing nutrient food by fermenting water oats with a Bacillus subtilis
4321258, Aug 13 1980 BOMA ENTERPRISES, INC Non-toxic insecticide
4323651, Dec 04 1974 R. J. Reynolds Tobacco Company Thermostable lactase derived from bacillus
4695546, Mar 06 1981 Shionogi & Co., Ltd. Transforming Bacillus stearothermophilus with plasmid vector pTB 19
4756913, Sep 30 1985 Sour milk product
4956177, Nov 04 1985 Microlife Technics, Inc. Method for inhibiting fungi
4980180, Jan 20 1990 SKW Trostberg Aktiengesellschaft Process for the removal of β-cyclodextrin from egg yolk or egg yolk plasma
5021344, Aug 31 1984 Centre National de la Recherche Scientifique (CNRS) Application of antibiotics of the phleomycin family as selection agent in the field of genetic engineering
5079164, Mar 10 1989 Jungbunzlauer Austria AG Microorganism of the species Bacillus ciaguans
5102800, Feb 04 1988 Rikagaku Kenkyusho Method for preparing novel cyclomaltodextrin gluccanotransferase
5176911, Aug 05 1988 ANIDRAL S R L Pharmaceutical compositions comprising selected lactobacillus strains
5200336, Jul 02 1990 New England Biolabs, Inc.; NEW ENGLAND BIOLABS, INC , A CORP OF MA Restriction endonuclease obtainable foam bacillus coagulans and a process for producing the same
5266315, Jul 05 1990 Kabushiki Kaisha Miyarisan Seibutsu Igaku Kenkyusho Composite for Clostridium difficile diarrhea and pseudomembranous colitis
5413960, May 01 1987 Biogaia Biologics AB Antibiotic reuterin
5439678, May 01 1987 Biogaia Biologics AB Method for inhibiting microorganism growth
5439995, Dec 22 1989 BP Chemicals Limited Catalyst and prepolymer used for the preparation of polyolefins
5531998, Dec 17 1987 United States Surgical Corporation Polycarbonate-based block copolymers and devices
5534253, Jun 07 1995 Biogaia Biologics AB Method of treating enteropathogenic bacterial infections in poultry
5665354, Jun 30 1994 Rutgers, The State University of New Jersey Bacillus licheniformis producing antifungal agents and uses thereof for control of phytopathogenic fungi
5785990, Jul 10 1995 MERRICK S, INC Feed fortifier and enhancer for preruminant calves and method of using same
5814319, Mar 22 1996 MITSUI NORIN CO , LTD Anti-viral, anti-bacterial and anti-cancer agent
5895672, Jan 13 1998 TEASHOT LLC Product and process for preparing a tea extract
5968569, Mar 19 1997 Nestec S A Pet food product containing probiotics
6080401, Nov 19 1998 REDDY, MALIREDDY S Herbal and pharmaceutical drugs enhanced with probiotics
6132710, Mar 17 1997 ProBiotix, Inc.; PROBIOTIX, INC Preventing/treating neonatal NEC by administering lactobacillus salivarius and lactobacillus plantarum or a combination thereof
6461607, Aug 24 1998 GANEDEN BIOTECH, INC Probiotic, lactic acid-producing bacteria and uses thereof
6531126, Aug 26 1999 Ganeden Biotech, Inc. Use of emu oil and its various fractions as a carrier for antifungal, antibacterial, and antiviral medications and preparations
6537543, Sep 14 2000 Unicafe Inc. Intestinal activation food using natto powder
6645506, Apr 18 1997 GANEDEN BIOTECH, INC Topical compositions containing extracellular products of Pseudomonas lindbergii and Emu oil
6706290, Jul 06 1998 CIFTCIOGLU, NEVA Methods for eradication of nanobacteria
6716435, Apr 18 1997 GANEDEN BIOTECH, INC Absorbent product containing absorbent structure and Bacillus coagulans
6723326, Apr 18 1997 Ganeden Biotech, Inc. Topical compositions containing probiotic Bacillus bacteria, spores, and extracellular products and uses thereof
6733751, Aug 26 1999 Ganeden Biotech, Inc. Use of Emu Oil and its various fractions as a carrier for antifungal, antibacterial, and antiviral medications & preparations
6811786, Apr 01 1999 GANEDEN BIOTECH, INC Methods for reducing cholesterol using Bacillus coagulans spores, systems and compositions
6835397, Dec 23 2002 Balchem Corporation Controlled release encapsulated bioactive substances
6849256, Nov 08 1999 Ganeden Biotech, Incorporated Inhibition of pathogens by probiotic bacteria
6905692, Apr 18 1997 Ganeden Biotech, Inc. Topical compositions containing probiotic bacillus bacteria, spores, and extracellular products and uses thereof
7024497, Sep 07 2000 Rovi Technologies Corporation Methods for accessing remotely located devices
7025974, Apr 18 1997 Ganeden Biotech Incorporated Absorbent product containing absorbent structure and bacillus coagulans
7048950, Aug 26 1999 Ganeden Biotech, Inc. Use of Emu Oil and its various fractions as a carrier for antifungal, antibacterial, and antiviral medications and preparations
7232571, Apr 01 1999 GANEDEN BIOTECH, INC Methods for reducing cholesterol using Bacillus coagulans spores, systems and compositions
7371407, Aug 26 1999 Ganeden Biotech, Inc. Use of Emu Oil and its various fractions as a carrier for antifungal, antibacterial, and antiviral medications and preparations
7374753, Jun 03 1997 Ganeden Biotech, Incorporated Probiotic lactic acid bacterium to treat bacterial infections associated with SIDS
7507402, Apr 10 1998 Ganeden Biotech, Incorporated Topical use of probiotic Bacillus spores to prevent or control microbial infections
7541042, Apr 18 1997 Ganeden Biotech, Inc. Topical compositions containing Bacillus coagulans extracellular products and uses thereof
7544363, Apr 18 1997 Ganeden Biotech, Inc. Topical compositions containing Bacillus coagulans extracellular products and uses thereof
7555715, Oct 25 2005 Rovi Product Corporation Methods and systems for use in maintaining media data quality upon conversion to a different data format
7700093, Dec 05 2003 GANEDEN BIOTECH, INC Methods for increasing lactose digestion
7708988, Aug 24 1998 Ganeden Biotech, Incorporated Probiotic, lactic acid-producing bacteria and uses thereof
7713726, Nov 08 1999 Ganeden Biotech Incorporated Inhibition of pathogens by probiotic bacteria
7767203, Aug 07 1998 GANEDEN BIOTECH, INC Methods for the dietary management of irritable bowel syndrome and carbohydrate malabsorption
7807151, Aug 24 1998 Ganeden Biotech, Incorporated Probiotic, lactic acid-producing bacteria and uses thereof
7807185, Apr 18 1997 Ganeden Biotech, Incorporated Methods of inhibiting growth of bacteria, yeast, fungus, and virus with Pseudomonas lindbergii and Bacillus coagulans extracellular products
7854927, May 11 2004 GANEDEN BIOTECH, INC Methods and compositions for the dietary management of autoimmune disorders
8097247, Aug 24 1998 Ganeden Biotech, Inc. Probiotic, lactic acid-producing bacteria and uses thereof
8187590, Aug 24 1998 Ganeden Biotech, Inc. Probiotic, lactic acid-producing bacteria and uses thereof
8273346, Aug 07 1998 Ganeden Biotech, Inc. Method for increasing fructose digestion with strains of Bacillus coagulans and fructase
8277799, Nov 08 1999 Ganeden Biotech, Incorporated Inhibition of pathogens by probiotic bacteria
8343484, Aug 07 1998 Ganeden Biotech, Inc. Methods for increasing lactose and fructose digestion
8349337, Apr 01 1999 Ganeden Biotech, Inc. Methods for reducing cholesterol using Bacillus coagulans spores, systems and compositions
8409591, May 11 2004 Ganeden Biotech, Inc. Methods and compositions for the dietary management of autoimmune disorders
8568743, Apr 29 2009 GANEDEN BIOTECH INC Inactivated bacterial cell formulation
8568744, Apr 29 2009 Ganeden Biotech, Inc. Inactivated bacterial cell formulation
8697055, Aug 24 1998 Ganeden Biotech, Inc. Probiotic, lactic acid-producing bacteria
8821854, Apr 18 1997 Ganeden Biotech, Inc. Methods for inhibiting microbial infections associated with sanitary products and for enhancing sanitary product degradation
9192659, Apr 29 2009 GANEDEN BIOTECH, INC Inactivated bacterial cell formulation
9220736, Aug 07 1998 Ganeden Biotech, Inc. Methods for the dietary management of irritable bowel syndrome and carbohydrate malabsorption
9301982, Apr 14 2010 GANEDEN BIOTECH, INC Probiotic confection and lipid compositions
9446111, Apr 29 2009 Ganeden Biotech, Inc. Inactivated bacterial cell formulation
9597286, Apr 14 2010 Ganeden Biotech, Inc. Probiotic confection and lipid compositions
9622502, Oct 16 2008 GANEDEN BIOTECH, INC Probiotic Bacillus pasta compositions
9757442, Apr 29 2009 Ganeden Biotech, Inc. Inactivated bacterial cell formulation
20030031659,
20030138936,
20030185811,
20040010510,
20040071685,
20040161522,
20040175459,
20040197277,
20050100535,
20050153040,
20050154682,
20050202145,
20050232909,
20050271643,
20060099197,
20060112584,
20060154350,
20060177429,
20060184538,
20060204633,
20070059400,
20080233104,
20080274153,
20080305096,
20090186057,
20090208606,
20090232941,
20100074993,
20100210000,
20110020305,
20110195154,
20110274676,
20120251512,
20130164398,
20130195824,
20130216577,
20130251695,
20130344046,
20140242051,
20150044317,
20150313951,
20160213612,
20160213613,
20160213614,
20160213615,
20170000872,
20170035813,
20170189331,
20170189457,
20170280755,
CA2606495,
CN1507812,
DE4132296,
EP1020123,
EP1344458,
EP1810579,
GB1040278,
JP10084845,
JP1084845,
JP11169145,
JP11335285,
JP2000093162,
JP2001252012,
JP2001286278,
JP2001292763,
JP2002502430,
JP2002522393,
JP2003513649,
JP2004337125,
JP2005137357,
JP2005536994,
JP2006025621,
JP2006254837,
JP2007000140,
JP2007044014,
JP2007054081,
JP2007082403,
JP2007537270,
JP2008013543,
JP4082827,
JP4158771,
JP45032905,
JP52136998,
JP5350399,
JP6166626,
JP64083025,
JP8175921,
JP9107869,
TW228974,
WO7606,
WO134168,
WO4004747,
WO4008870,
WO5092122,
WO5110445,
WO8112296,
WO9029267,
WO9051753,
WO2005019417,
WO2005055934,
WO2005117926,
WO2006007470,
WO2006090729,
WO2007012847,
WO2007058027,
WO8905849,
WO9314187,
WO9400019,
WO9411492,
WO9611014,
WO9729762,
WO9734615,
WO9854982,
/////////
Executed onAssignorAssigneeConveyanceFrameReelDoc
Aug 27 2008Ganeden Biotech, Inc.(assignment on the face of the patent)
Mar 12 2009FARMER, SEANGANEDEN BIOTECH INC ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0224460672 pdf
Mar 12 2009LEFKOWITZ, ANDREW R GANEDEN BIOTECH INC ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0224460672 pdf
Mar 12 2009BUSH, MICHAELGANEDEN BIOTECH INC ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0224460672 pdf
Mar 12 2009MASKE, DAVIDGANEDEN BIOTECH INC ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0224460672 pdf
Jun 01 2011GANEDEN BIOTECH, INC SCHIFF NUTRITION GROUP, INC LICENSE SEE DOCUMENT FOR DETAILS 0266160128 pdf
Jun 01 2011GANEDEN BIOTECH, INC SCHIFF NUTRITION GROUP, INC SECURITY AGREEMENT0266160950 pdf
Oct 05 2012GANEDEN BIOTECH, INC Silicon Valley BankSECURITY AGREEMENT0291030069 pdf
Aug 31 2017Silicon Valley BankGANEDEN BIOTECH, INC RELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0438220897 pdf
Date Maintenance Fee Events
Jan 25 2023M1551: Payment of Maintenance Fee, 4th Year, Large Entity.


Date Maintenance Schedule
Aug 20 20224 years fee payment window open
Feb 20 20236 months grace period start (w surcharge)
Aug 20 2023patent expiry (for year 4)
Aug 20 20252 years to revive unintentionally abandoned end. (for year 4)
Aug 20 20268 years fee payment window open
Feb 20 20276 months grace period start (w surcharge)
Aug 20 2027patent expiry (for year 8)
Aug 20 20292 years to revive unintentionally abandoned end. (for year 8)
Aug 20 203012 years fee payment window open
Feb 20 20316 months grace period start (w surcharge)
Aug 20 2031patent expiry (for year 12)
Aug 20 20332 years to revive unintentionally abandoned end. (for year 12)